8 results match your criteria: "Medical laboratory of Shenzhen Luohu Hospital Group[Affiliation]"

Massilia shenzhen sp. nov., isolated from blood of one premature infant, causing sepsis.

Diagn Microbiol Infect Dis

January 2025

School of Medicine, Anhui University of Science and Technology, 168 Taifeng Road, 232000 Huainan, PR China; Department of Medical Laboratory, The University of Hong Kong - Shenzhen Hospital, 518053, PR China. Electronic address:

Article Synopsis
  • - The study focuses on a premature infant suffering from pneumonia and respiratory failure, characteristic of neonatal sepsis, where blood tests eventually identified a pathogen after initial tests were negative.
  • - Advanced methods like MALDI-TOF-MS and whole genome sequencing led to the identification of the pathogen as a new species, Massilia shenzhen sp. nov., with specific physical and genetic traits detailed in the research.
  • - The pathogen showed susceptibility to antibiotics, with low minimum inhibitory concentrations for ceftazidime and imipenem, suggesting potential treatment options for infections caused by Massilia, although drug resistance research is limited.
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Background: In bladder cancer, recurrent ADGRG6 enhancer hotspot mutations (chr. 6: 142,706,206 G>A, chr. 6:142,706,209 C>T) were reported at a high mutation rate of approximately 50%.

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A rapid multiplex assay of human malaria parasites by digital PCR.

Clin Chim Acta

January 2023

Department of Laboratory Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China. Electronic address:

Background: Blood smear examination through traditional optical microscopy is the gold standard for malaria diagnosis. However, it imposes strict requirements for operational staff and its sensitivity cannot perfectly satisfy the needs of clinical requirements. More sensitive and accurate modern technologies should be applied to this field.

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The Sanger sequencing techniques, also known as the first-generation sequencing techniques and the gold standard of sequencing, have promoted the completion of "working draft" of the human genome, but the disadvantages of low throughput and high cost limit its large-scale application. The second-generation sequencing techniques, also known as the next-generation sequencing techniques, have widely used in basic research and clinical application because of its high throughput and low cost, but the short reads has always been an unavoidable shortcoming. Then, the emergence of the third-generation sequencing techniques, with the long reads, provides new technology selection for the analysis of complex repetitive regions on genome sequences and the assembly of high-quality genomes.

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Purpose: To investigated the changes of gut microbiome and fecal metabolome during anti-tuberculosis chemotherapy with isoniazid (H)-rifampin (R)-pyrazinamide (Z)-ethambutol (E).

Patients And Methods: (1) In this study, we recruited 168 stool specimens from 49 healthy volunteers without (Mtb), 30 healthy volunteers with latently infected by Mtb, 41 patients with active tuberculosis (ATB), 28 patients with 2-month HRZE treatment and 20 patients with 2-month HRZE followed by 4-month HR treatment. (2) We used 16S rRNA sequencing and an untargeted Liquid Chromatograph Mass Spectrometer-based metabolomics to investigate the changes of gut microbiome and the alteration of fecal metabolome, respectively, during anti-TB chemotherapy.

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Autoantibodies are currently the most robust biomarkers of type 1 diabetes. However, single autoantibody targeted detection is still limited in diabetes diagnosis with poor performance. Here, we develop a multiplexed Array-ELISA assay that can detect five diabetes-related autoantibodies including glutamic acid decarboxylase antibody (GADA), insulinoma antigen 2 antibody (IA-2A), islet cell antibody (ICA), zinc transporter 8 autoantibody (ZnT8-A) and insulin antibody (IAA) simultaneously.

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Background: Currently, mass vaccine inoculation against coronavirus disease-2019 (COVID-19) has been being implemented globally. Rapid and the large-scale detection of serum neutralizing antibodies (NAbs) laid a foundation for assessing the immune response against SARS-CoV-2 infection and vaccine. Additional assessments include the duration of antibodies and the optimal time for a heightened immune response.

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Background: Seldom performance evaluation and diagnosis comparison studies were reported for different chemiluminescent immunoassay (CLIA) kits approved under an emergency approval program for SARS-CoV-2 infection.

Methods: A total of 100 and 105 serum separately from non-infected populations and COVID-19 patients were detected with SARS-CoV-2 IgM and IgG kits. The characteristics including precision, functional sensitivity, linearity, and accuracy were evaluated for Axceed, iFlash, and Maglumi CLIA kits.

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